Oakes Vanessa, Wang Weili, Harrington Brittney, Lee Won Jae, Beamish Heather, Chia Kee Ming, Pinder Alex, Goto Hidemasa, Inagaki Masaki, Pavey Sandra, Gabrielli Brian
a The University of Queensland Diamantina Institute; Translational Research Institute ; Brisbane , Queensland , Australia.
Cell Cycle. 2014;13(20):3302-11. doi: 10.4161/15384101.2014.949111.
Whereas many components regulating the progression from S phase through G2 phase into mitosis have been identified, the mechanism by which these components control this critical cell cycle progression is still not fully elucidated. Cyclin A/Cdk2 has been shown to regulate the timing of Cyclin B/Cdk1 activation and progression into mitosis although the mechanism by which this occurs is only poorly understood. Here we show that depletion of Cyclin A or inhibition of Cdk2 during late S/early G2 phase maintains the G2 phase arrest by reducing Cdh1 transcript and protein levels, thereby stabilizing Claspin and maintaining elevated levels of activated Chk1 which contributes to the G2 phase observed. Interestingly, the Cyclin A/Cdk2 regulated APC/C(Cdh1) activity is selective for only a subset of Cdh1 targets including Claspin. Thus, a normal role for Cyclin A/Cdk2 during early G2 phase is to increase the level of Cdh1 which destabilises Claspin which in turn down regulates Chk1 activation to allow progression into mitosis. This mechanism links S phase exit with G2 phase transit into mitosis, provides a novel insight into the roles of Cyclin A/Cdk2 in G2 phase progression, and identifies a novel role for APC/C(Cdh1) in late S/G2 phase cell cycle progression.
尽管已经鉴定出许多调节从S期经G2期进入有丝分裂进程的组分,但这些组分控制这一关键细胞周期进程的机制仍未完全阐明。细胞周期蛋白A/细胞周期蛋白依赖性激酶2(Cyclin A/Cdk2)已被证明可调节细胞周期蛋白B/细胞周期蛋白依赖性激酶1(Cyclin B/Cdk1)的激活时间和进入有丝分裂的进程,尽管其发生机制仍知之甚少。在这里,我们表明,在S期末期/ G2期早期耗尽细胞周期蛋白A或抑制Cdk2,可通过降低Cdh1转录本和蛋白水平来维持G2期阻滞,从而稳定Claspin并维持活化的Chk1的高水平,这促成了所观察到的G2期。有趣的是,细胞周期蛋白A/Cdk2调节的后期促进复合物/ Cdh1(APC/C(Cdh1))活性仅对包括Claspin在内的Cdh1靶标的一个子集具有选择性。因此,细胞周期蛋白A/Cdk2在G2期早期的正常作用是增加Cdh1的水平,Cdh1会使Claspin不稳定,而Claspin又会下调Chk1的激活,从而允许进入有丝分裂。这种机制将S期退出与G2期向有丝分裂的转变联系起来,为细胞周期蛋白A/Cdk2在G2期进程中的作用提供了新的见解,并确定了后期促进复合物/ Cdh(APC/C(Cdh1))在S期末期/ G2期细胞周期进程中的新作用。